(+/-)-Narwedine丨CAS 1668-86-6

(+/-)-Narwedine丨CAS 1668-86-6
Product Introduction:
Catalog No.: SS130552
CAS No.: 1668-86-6
Purity(HPLC): 98.0% min
Product Name: (+/-)-Narwedine
Molecular Formula: C17H19NO3
Molecular Weight: 285.34
Synonym(s): (+/-)-3-Deoxy-3-oxogalanthamine; DL-Narwedine
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Technical Parameters
Description

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Specifications

 

Appearance: White or off-white powder
Purity(HPLC): 98.0% min
Heavy metal: 20ppm max
Loss on drying: 1.0% max
Related substances (HPLC):  
Single impurities: 1.0% max
Total impurities: 2.0% max

 

 

 

Applications

 

(+/-)-Narwedine is most prominently utilized as a key intermediate in the synthesis of galanthamine hydrobromide, an acetylcholinesterase inhibitor approved for the treatment of Alzheimer's disease and other cognitive impairments. Its structural features make it an essential building block in both natural product synthesis and semisynthetic production routes for alkaloid-based drugs. In pharmaceutical research, it is used to explore stereoselective and asymmetric synthesis techniques, contributing to the development of chiral drug molecules with improved efficacy and safety profiles. The compound also finds use in academic and industrial laboratories for mechanistic studies, enantioselective catalysis, and the development of green chemistry synthesis strategies. Beyond drug synthesis, (+/-)-Narwedine plays a role in biochemical studies investigating neuroactive compounds derived from Amaryllidaceae alkaloids. Its versatile reactivity enables it to serve as a model compound in exploring oxidative coupling reactions and intramolecular rearrangements, making it a valuable research material for synthetic chemists.

 

Benefits

 

The main benefit of (+/-)-Narwedine lies in its versatility and pharmaceutical relevance. As a direct precursor to galanthamine, it enables efficient and scalable synthesis pathways that support the growing global demand for Alzheimer's treatments. Its well-defined structure allows for controlled stereochemical manipulation, helping chemists design optimized routes to produce both racemic and enantiomerically pure products. The compound's chemical stability, predictable reactivity, and compatibility with modern synthetic methods make it a reliable intermediate for both laboratory-scale and industrial-scale operations. Additionally, the use of (+/-)-Narwedine in research facilitates the discovery of new analogs with potential neuroprotective and anti-inflammatory properties, thereby advancing the field of neuropharmacology. Its contribution to sustainable synthesis approaches-through reduced reaction steps and environmentally friendly reagents-further underscores its importance in modern medicinal chemistry.

 

Conclusion

 

In conclusion, (+/-)-Narwedine is a critical compound in the pharmaceutical and chemical research industries, serving as a cornerstone intermediate in the synthesis of galanthamine and other bioactive alkaloids. Its structural precision, chemical stability, and synthetic adaptability make it indispensable in both practical drug production and theoretical research. As interest in efficient and eco-conscious synthesis methods continues to rise, (+/-)-Narwedine remains a key enabler for innovation in alkaloid chemistry, neurotherapeutic development, and advanced organic synthesis.

 

 

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